Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Avidin-biotin-DOTA-90Y is an investigational, two-component pretargeted radionuclide therapy (PRT) system designed for the treatment of nonpalpable (occult) breast cancer. The therapy utilizes a sequential intralesional administration strategy: first, native avidin is injected at the tumor site (following vacuum-assisted biopsy), where it serves as an interstitial molecular anchor due to its high retention in the tissue. Subsequently, yttrium-90-labeled DOTA-biotin (90Y-DOTA-biotin) is administered locally. The extremely high affinity between avidin and biotin ensures that the radioactive payload binds tightly to the anchored avidin, delivering targeted beta radiation directly to the malignant lesion while minimizing systemic exposure. This approach is being evaluated in the Phase 1 ARTHE trial to assess safety and anti-tumor activity in patients with occult infiltrating breast cancer.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on avidin + yttrium-90-DOTA-biotin (Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori").